Vancomycin Hydrochloride
- Product NDC
- 68001-338
- 11-digit product format
- 680010338
- Labeler code
- 68001
- Product ID
- 68001-338_c91fb4b4-7b6c-c700-e053-2995a90a6bc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vancomycin
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- ANDA205694
- Marketing category
- ANDA
- Marketing start
- 2018-01-31
- Marketing end
- 2022-06-30
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC],Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-338-62 | 68001033862 | 10 VIAL, SINGLE-USE in 1 CARTON (68001-338-62) > 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-USE (68001-338-61) | 2018-01-31 | 0000-00-00 | No | No | Current |